Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use: 1-3 capsules per day with meals, Distr
Summary
The FDA issued a Class II for Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use by Veridance Pharmacal, LLC. Reason: Levels of iodine exceeding label claim.
Details
Source
Food Recall
External ID
F-0671-2025
Action Date
2025-04-02
Status
Terminated
Category
food
Product Description
Omni-Macs McDonagh Medical Center Dietary Supplement 100 CAPSULES, Suggested Use: 1-3 capsules per day with meals, Distributed by: McDonagh Medical Center Gladstone, MO 64119
Lot/Code Info: UPC: 850038221294, Lot codes: 0311-01 exp. 3/26, 0311-02 exp. 3/26, 0367-01 exp. 8/26
Quantity Affected: 450 bottles
Reason for Recall
Levels of iodine exceeding label claim
Distribution
One customer located in Gladstone, MO
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-10
Company
Springdale, AR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Veridance Pharmacal, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Veridance Pharmacal, LLC have FDA actions?
This is the only FDA action we have on record for Veridance Pharmacal, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0671-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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